Ivaturi V D, Riss J R, Kriel R L, Cloyd J C
Center for Orphan Drug Research, University of Minnesota, Minnesapolis, MN 55455, USA.
Acta Neurol Scand. 2009 Nov;120(5):353-7. doi: 10.1111/j.1600-0404.2009.01170.x. Epub 2009 May 14.
The purpose of this pilot study was to determine the pharmacokinetics and tolerability of an investigational diazepam (DZP) formulation and a parenteral midazolam (MDZ) formulation following intranasal (i.n.) administration for the efficient treatment of seizure emergencies.
Each subject received 5 mg of DZP and MDZ via both i.n. and intravenous routes in a four-way, randomized crossover trial. Blood samples were collected over 48 h. DZP and MDZ concentrations were measured using HPLC. Using analog scales, subjects rated tolerability (0 = no change from normal; 10 = maximum intolerability) and pain (0 = no pain; 4 = extreme pain) prior to and 0, 5, 15, 60 min, and 8 h after administration.
The C(max) and T(max) values for i.n. DZP and MDZ were 179.2 ng/ml and 28.8 min vs 62.8 ng/ml and 21.6 min, respectively. Immediately following i.n. administration, subjects reported tolerability scores of 6.75 and 6.0, and identical pain scores, 3.2, for DZP and MDZ, respectively.
Both formulations were rapidly absorbed following i.n. administration with transient discomfort. DZP had a longer half-life, which may result in an extended duration of action. Further studies in large patient populations to evaluate the safety after long term use, efficacy and pharmacokinetics of i.n. DZP are warranted.
本初步研究旨在确定一种试验性地西泮(DZP)制剂和一种胃肠外咪达唑仑(MDZ)制剂经鼻内(i.n.)给药后用于有效治疗癫痫紧急情况的药代动力学和耐受性。
在一项四路随机交叉试验中,每位受试者通过鼻内和静脉途径接受5mg的DZP和MDZ。在48小时内采集血样。使用高效液相色谱法(HPLC)测量DZP和MDZ的浓度。受试者在给药前以及给药后0、5、15、60分钟和8小时使用模拟量表对耐受性(0 = 与正常无变化;10 = 最大不耐受)和疼痛(0 = 无疼痛;4 = 极度疼痛)进行评分。
鼻内给予DZP和MDZ的C(max)和T(max)值分别为179.2 ng/ml和28.8分钟,以及62.8 ng/ml和21.6分钟。鼻内给药后,受试者报告DZP和MDZ的耐受性评分分别为6.75和6.0,疼痛评分相同,均为3.2。
两种制剂经鼻内给药后均迅速吸收,伴有短暂不适。DZP的半衰期更长,这可能导致作用持续时间延长。有必要对大量患者群体进行进一步研究,以评估长期使用后鼻内给予DZP的安全性、疗效和药代动力学。